Anaerobic dissolved As(III) removal from metalpolluted waters by cathode-stabilized Fe(III)- oxyhydroxides.
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F23%3A00571472" target="_blank" >RIV/60077344:_____/23:00571472 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/60076658:12310/23:43907569 RIV/00025798:_____/23:10168739
Výsledek na webu
<a href="https://pubs.rsc.org/en/content/articlelanding/2023/EW/D2EW00844K" target="_blank" >https://pubs.rsc.org/en/content/articlelanding/2023/EW/D2EW00844K</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/d2ew00844k" target="_blank" >10.1039/d2ew00844k</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Anaerobic dissolved As(III) removal from metalpolluted waters by cathode-stabilized Fe(III)- oxyhydroxides.
Popis výsledku v původním jazyce
A bioelectrochemical system (BES) to efficiently induce arsenite scavenging from anoxic waters is yet to be developed. Here we examined to what extent the presence of redox reactive humic substances derivatives and reactive nitrogen species interferes with the bioelectrochemically induced immobilization of As(iii) by Fe(iii) oxyhydroxides. Insights from extracellular electron transfer to insoluble minerals by a strain of Geobacter sp. were acquired and integrated with data from acetate utilization. We furthered our interpretations with in situ synchrotron-based analyses of experimentally precipitated biominerals. Geobacter sp. cells interacting with cathodes used oxidized humic substance derivatives as electron shuttles which fostered the partial reduction of Fe(iii), thus promoting the scavenging of As(iii) oxyanions. The oxyanions became immobilized in the reactive surfaces of FeOOH within mineral aggregates, where they were readily oxidized presumably as the result of related Fenton-like reactions. An experiment lacking humic derivatives fueled the formation of bacterial-mineral networks. These networks fostered short-range electron transfer mechanisms that initially promoted biotic amorphous ferrihydrite aggregation. The early ferrihydrite aggregates exhibited a decreased As(iii) scavenging capacity. In the presence of both humic derivatives and ammonium, the proposed BES was proven more effective in removing As(iii) from solution and despite elevated competing phosphate levels. In the presence of reactive N species alone, stabilization of Fe(iii) and microbial attachment promoted Fe(ii) scavenging which outcompeted As(iii) from the available ligands in the reactive mineral surfaces. Improving mineral stabilization is deemed crucial for direct As(iii)-sequestration in BESs. An optimized BES for As-removal would be beneficial not only for sequestering arsenite out of solution in geogenically polluted aqueous systems, but also for addressing the recurrent eutrophication of continental water bodies linked to seasonal phosphate solubilization.
Název v anglickém jazyce
Anaerobic dissolved As(III) removal from metalpolluted waters by cathode-stabilized Fe(III)- oxyhydroxides.
Popis výsledku anglicky
A bioelectrochemical system (BES) to efficiently induce arsenite scavenging from anoxic waters is yet to be developed. Here we examined to what extent the presence of redox reactive humic substances derivatives and reactive nitrogen species interferes with the bioelectrochemically induced immobilization of As(iii) by Fe(iii) oxyhydroxides. Insights from extracellular electron transfer to insoluble minerals by a strain of Geobacter sp. were acquired and integrated with data from acetate utilization. We furthered our interpretations with in situ synchrotron-based analyses of experimentally precipitated biominerals. Geobacter sp. cells interacting with cathodes used oxidized humic substance derivatives as electron shuttles which fostered the partial reduction of Fe(iii), thus promoting the scavenging of As(iii) oxyanions. The oxyanions became immobilized in the reactive surfaces of FeOOH within mineral aggregates, where they were readily oxidized presumably as the result of related Fenton-like reactions. An experiment lacking humic derivatives fueled the formation of bacterial-mineral networks. These networks fostered short-range electron transfer mechanisms that initially promoted biotic amorphous ferrihydrite aggregation. The early ferrihydrite aggregates exhibited a decreased As(iii) scavenging capacity. In the presence of both humic derivatives and ammonium, the proposed BES was proven more effective in removing As(iii) from solution and despite elevated competing phosphate levels. In the presence of reactive N species alone, stabilization of Fe(iii) and microbial attachment promoted Fe(ii) scavenging which outcompeted As(iii) from the available ligands in the reactive mineral surfaces. Improving mineral stabilization is deemed crucial for direct As(iii)-sequestration in BESs. An optimized BES for As-removal would be beneficial not only for sequestering arsenite out of solution in geogenically polluted aqueous systems, but also for addressing the recurrent eutrophication of continental water bodies linked to seasonal phosphate solubilization.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10503 - Water resources
Návaznosti výsledku
Projekt
<a href="/cs/project/GJ19-15096Y" target="_blank" >GJ19-15096Y: Souběžné mikrobiálně řízené cykly železa, dusíku a fosforu a jejich přechodové oddělení v vodních ekosystémech bohatých na redukované železo</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2023
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Environmental Science-Water Research & Technology
ISSN
2053-1400
e-ISSN
2053-1419
Svazek periodika
9
Číslo periodika v rámci svazku
2
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
13
Strana od-do
454-466
Kód UT WoS článku
000897894400001
EID výsledku v databázi Scopus
2-s2.0-85144807061